HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms

MessageThis Webinar is over
Date Jul 10, 2018
Time 1:00 pm to 2:00 pm
Cost 13420.00
Online
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity and personnel is crucial to protect the product from contamination.
Therefore, the design, validation and ongoing monitoring of a clean room HVAC system is necessary to assure the quality and safety of the pharmaceutical product.

Why You Should Attend:
This webinar first details and explains the various US and international regulatory requirements for various clean room classifications.
Next, the webinar provides a comprehensive overview of the mechanics of clean room HVAC. This includes engineering diagrams and schematics. HVAC equipment components are detailed as well as the automated control systems that are available. Clean room design considerations are included. Proper building construction and layout is necessary to achieve both optimum efficiency of the system and optimum cleaning and sanitization of the clean room.

Areas Covered in the Session :
  • GMP Compliance of Clean Room Environment
  • Regulatory Clean Room Classification and Requirements
  • HVAC System Components
  • Clean Room Design and Layout
  • HEPA Filtration
  • Differential Pressure and Air Pressure Balancing Considerations
  • Temperature and Humidity Controls
  • Cleaning and Disinfection
  • Personnel Gowning and Aseptic Practices in Clean Room
  • HVAC System Validation

Who Will Benefit:
  • Quality Assurance Departments
  • Environmental Monitoring Departments
  • Microbiology Departments
  • Manufacturing Departments
  • Validation Departments
  • Engineering Departments
  • Maintenance Departments

 


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